A Probabilistic Approach for the Evaluation of Minimal Residual Disease by Multiparameter Flow Cytometry in Leukemic B-Cell Chronic Lymphoproliferative Disorders

被引:53
作者
Pedreira, C. E. [1 ,2 ]
Costa, E. S. [3 ,4 ]
Almeida, J. [5 ,6 ]
Fernandez, C. [5 ,6 ]
Quijano, S. [5 ,6 ]
Flores, J. [5 ,6 ]
Barrena, S. [5 ,6 ]
Lecrevisse, Q. [5 ,6 ]
Van Dongen, J. J. M. [7 ]
Orfao, A. [5 ,6 ]
机构
[1] Univ Fed Rio de Janeiro, Fac Med, Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, COPPE, PEE, Engn Grad Program, BR-21945 Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, IPPMG, Rio De Janeiro, Brazil
[4] Univ Fed Rio de Janeiro, Dept Clin Med, Rio De Janeiro, Brazil
[5] Univ Salamanca, Cytometry Serv, Dept Med, E-37008 Salamanca, Spain
[6] Univ Salamanca, Canc Res Ctr, IBMCC, CSIC, E-37008 Salamanca, Spain
[7] Univ Med Ctr Rotterdam, Erasmus MC, Dept Immunol, Rotterdam, Netherlands
关键词
minimal residual disease; flow cytometry; principal component analysis; pattern classification; leukemia; Bayes theorem;
D O I
10.1002/cyto.a.20638
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Multiparameter flow cytometry has become an essential too] for monitoring response to therapy in hematological malignancies, including B-cell chronic lymphoproliferative disorders (B-CLPD). However, depending on the expertise of the operator minimal residual disease (MRD) can be misidentified, given that data analysis is based on the definition of expert-based bidimensional plots, where an operator selects the subpopulations of interest. Here, we propose and evaluate a probabilistic approach based on pattern classification tools and the Bayes theorem, for automated analysis of flow cytometry data from a group of 50 B-CLPD versus normal peripheral blood B-cells under MRD conditions, with the aim of reducing operator-associated subjectivity. The proposed approach provided a tool for MRD detection in B-CLPD by flow cytometry with a sensitivity of <= 8 x 10(-5) (median of <= 2 x 10(-7)). Furthermore, in 86% of BCLPD cases tested, no events corresponding to normal B-cells were wrongly identified as belonging to the neoplastic B-cell population at a level of <= 10(-7). Thus, this approach based on the search for minimal numbers of neoplastic B-cells similar to those detected at diagnosis could potentially be applied with both a high sensitivity and specificity to investigate for the presence of MRD in virtually all B-CLPD. Further studies evaluating its efficiency in larger series of patients, where reactive conditions and non-neoplastic disorders are also included, are required to confirm these results. (C) 2008 International Society for Advancement of Cytometry
引用
收藏
页码:1141 / 1150
页数:10
相关论文
共 42 条
[1]   A segmental maximum a posteriori approach to genome-wide copy number profiling [J].
Andersson, Robin ;
Bruder, Carl E. G. ;
Piotrowski, Arkadiusz ;
Menzel, Uwe ;
Nord, Helena ;
Sandgren, Johanna ;
Hvidsten, Torgeir R. ;
de Stahl, Teresita Diaz ;
Dumanski, Jan P. ;
Komorowski, Jan .
BIOINFORMATICS, 2008, 24 (06) :751-758
[2]   A new automated flow cytometry data analysis approach for the diagnostic screening of neoplastic B-cell disorders in peripheral blood samples with absolute lymphocytosis [J].
Costa, E. S. ;
Arroyo, M. E. ;
Pedreira, C. E. ;
Garcia-Marcos, M. A. ;
Tabernero, M. D. ;
Almeida, J. ;
Orfao, A. .
LEUKEMIA, 2006, 20 (07) :1221-1230
[3]   Clinical importance of minimal residual disease in childhood acute lymphoblastic leukemia [J].
Coustan-Smith, E ;
Sancho, J ;
Hancock, ML ;
Boyett, JM ;
Behm, FG ;
Raimondi, SC ;
Sandlund, JT ;
Rivera, GK ;
Rubnitz, JE ;
Ribeiro, RC ;
Pui, CH ;
Campana, D .
BLOOD, 2000, 96 (08) :2691-2696
[4]   2006 Bethesda international consensus recommendations on the flow cytometric immunophenotypic analysis of hematolymphoid neoplasia: Medical indications [J].
Davis, B. H. ;
Holden, J. T. ;
Bene, M. C. ;
Borowitz, M. J. ;
Braylan, R. C. ;
Cornfield, D. ;
Gorczyca, W. ;
Lee, R. ;
Maiese, R. ;
Orfao, A. ;
Wells, D. ;
Wood, B. L. ;
Stetler-Stevenson, M. .
CYTOMETRY PART B-CLINICAL CYTOMETRY, 2007, 72B :S5-S13
[5]  
Duda R.O., 2001, PATTERN CLASSIFICATI, p[36, 174, 517, 20]
[6]  
DUDA RO, 2001, PATTERN CLASSIFICATI, P115
[7]   Flow cytometry for high-throughput, high-content screening [J].
Edwards, BS ;
Oprea, T ;
Prossnitz, ER ;
Sklar, LA .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2004, 8 (04) :392-398
[8]   ALEXA: a microarray design platform for alternative expression analysis [J].
Griffith, Malachi ;
Tang, Michelle J. ;
Griffith, Obi L. ;
Morin, Ryan D. ;
Chan, Susanna Y. ;
Asano, Jennifer K. ;
Zeng, Thomas ;
Flibotte, Stephane ;
Ally, Adrian ;
Baross, Agnes ;
Hirst, Martin ;
Jones, Steven J. M. ;
Morin, Gregg B. ;
Tai, Isabella T. ;
Marra, Marco A. .
NATURE METHODS, 2008, 5 (02) :118-118
[9]   World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: Report of the Clinical Advisory Committee Meeting - Airlie House, Virginia, November 1997 [J].
Harris, NL ;
Jaffe, ES ;
Diebold, J ;
Flandrin, G ;
Muller-Hermelink, HK ;
Vardiman, J ;
Lister, TA ;
Bloomfield, CD .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (12) :3835-3849
[10]   Monitoring of minimal residual disease in acute myeloid leukemia [J].
Kern, Wolfgang ;
Haferlach, Claudia ;
Haferlach, Torsten ;
Schnittger, Susanne .
CANCER, 2008, 112 (01) :4-16